rs374615369

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs374615369(C;T)

Make rs374615369(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

178774305

Gene

TTN

is a	snp
is	mentioned by
dbSNP	rs374615369
dbSNP (classic)	rs374615369
ClinGen	rs374615369
ebi	rs374615369
HLI	rs374615369
Exac	rs374615369
Gnomad	rs374615369
Varsome	rs374615369
LitVar	rs374615369
Map	rs374615369
PheGenI	rs374615369
Biobank	rs374615369
1000 genomes	rs374615369
hgdp	rs374615369
ensembl	rs374615369
geneview	rs374615369
scholar	rs374615369
google	rs374615369
pharmgkb	rs374615369
gwascentral	rs374615369
openSNP	rs374615369
23andMe	rs374615369
SNPshot	rs374615369
SNPdbe	rs374615369
MSV3d	rs374615369
GWAS Ctlg	rs374615369

Max Magnitude

0

ClinVar
Risk	rs374615369(T;T)
Alt	rs374615369(T;T)
Reference	Rs374615369(C;C)
Significance	Probable-Pathogenic
Disease	not provided Dilated cardiomyopathy 1G Limb-girdle muscular dystrophy
Variation	info
Gene	TTN
CLNDBN	not provided Dilated cardiomyopathy 1G Limb-girdle muscular dystrophy, type 2J
Reversed	0
HGVS	NC_000002.11:g.179639032C>T
CLNSRC
CLNACC	RCV000171324.1, RCV000473786.1,